Brock James A, Tan Joy H C
Prince of Wales Medical Research Institute, University of New South Wales, Barker Street, Randwick NSW 2031, Australia.
Br J Pharmacol. 2004 May;142(2):267-74. doi: 10.1038/sj.bjp.0705779.
The effects of blocking alpha(2)-adrenoceptors on noradrenaline (NA) and adenosine 5'-triphosphate (ATP) release from postganglionic sympathetic nerves have been investigated in rat-tail artery in vitro. Continuous amperometry was used to measure NA release and intracellularly recorded excitatory junction potentials (e.j.p.'s) were used to measure ATP release. Application of the alpha(2)-adrenoceptor antagonist, idazoxan (1 microm), increased the amplitude of NA-induced oxidation currents evoked by trains of 10 stimuli at 1 and 10 Hz. In cells deep in the media, idazoxan (1 microm) had no effect on the amplitude of e.j.p.'s evoked by trains of 10 stimuli at 1 and 10 Hz. In cells close to the adventitial - medial border, idazoxan produced a small increase in the amplitude of e.j.p.'s evoked at the end of trains of 10 stimuli at 1 Hz. In tissues pretreated with the neuronal NA uptake inhibitor, desmethylimpramine (0.3 microm), idazoxan (1 microm) markedly increased the amplitude of e.j.p.'s in cells deep in the media. The alpha(2)-adrenoceptor agonist, clonidine (0.5 microm), produced similar reductions in the amplitudes of both NA-induced oxidation currents and e.j.p.'s evoked by 10 stimuli at 1 Hz. These effects of clonidine were reversed by the subsequent addition of idazoxan (1 microm). The release of both NA and ATP is inhibited to a similar extent by activation of prejunctional alpha(2)-adrenoceptors by clonidine. In contrast, endogenously released NA more markedly inhibits NA release. These findings provide further support for the differential modulation of NA and ATP release.
在体外大鼠尾动脉中研究了阻断α₂ - 肾上腺素能受体对节后交感神经去甲肾上腺素(NA)和5'-三磷酸腺苷(ATP)释放的影响。采用连续安培法测量NA释放,并用细胞内记录的兴奋性接头电位(e.j.p.)测量ATP释放。应用α₂ - 肾上腺素能受体拮抗剂咪唑克生(1 μmol),可增加1 Hz和10 Hz频率下10次刺激串诱发的NA诱导氧化电流的幅度。在中膜深层的细胞中,咪唑克生(1 μmol)对1 Hz和10 Hz频率下10次刺激串诱发的e.j.p.幅度无影响。在靠近外膜 - 中膜边界的细胞中,咪唑克生使1 Hz频率下10次刺激串结束时诱发的e.j.p.幅度略有增加。在用神经元NA摄取抑制剂去甲丙咪嗪(0.3 μmol)预处理的组织中,咪唑克生(1 μmol)显著增加了中膜深层细胞中e.j.p.的幅度。α₂ - 肾上腺素能受体激动剂可乐定(0.5 μmol)对1 Hz频率下10次刺激诱发的NA诱导氧化电流幅度和e.j.p.幅度产生类似的降低作用。随后加入咪唑克生(1 μmol)可逆转可乐定的这些作用。可乐定激活节前α₂ - 肾上腺素能受体对NA和ATP的释放均有相似程度的抑制作用。相比之下,内源性释放的NA对NA释放的抑制作用更为明显。这些发现为NA和ATP释放的差异调节提供了进一步的支持。